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Symbol
Name
ID

Hnrnph2
heterogeneous nuclear ribonucleoprotein H2
MGI:1201779

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes

Micrognathia

Secondary microcephaly

Midface retrusion

Short philtrum

Thick vermilion border

High palate

Wide mouth

Drooling

Low hanging columella

Underdeveloped nasal alae

Almond-shaped palpebral fissure

Short palpebral fissure

Epicanthus

Disease(s) Associated with HNRNPH2

syndromic X-linked intellectual developmental disorder bain type

Mouse Phenotypes		abnormal craniofacial morphology	decreased cranium height	short mandible	short maxilla	domed cranium	short snout
Availability	Mouse Genotype	abnormal craniofacial morphology	decreased cranium height	short mandible	short maxilla	domed cranium	short snout
	Hnrnph2^em1(IMPC)J/Hnrnph2^em1(IMPC)J
	Hnrnph2^em1Jpat/Hnrnph2⁺
	Hnrnph2^em1Jpat/Y
	Hnrnph2^em2Jpat/Y
	Hnrnph2^em3Jpat/Y

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/14/2024 MGI 6.23